BACKGROUND
[0001] The present disclosure relates generally to barrier coatings for metal substrates
and, more particularly, to non-hexavalent chromium chemical conversion coatings (CCCs)
and the application thereof.
[0002] Aluminum and aluminum alloy components used in aeronautics and aerospace applications
are subjected to environments that cause corrosion. MIL-DTL-81706 Type II CCCs are
used to form a corrosion-resistant protective barrier coating by reaction with the
surface of aluminum and aluminum alloy substrates. Type II refers to compositions
containing no hexavalent chromium, which has been banned in many countries. Repair
of these barrier coatings is often required over the operational life of a component.
On-wing repair is preferred but has associated challenges related to spatial constraints
and the orientation of surfaces requiring repair. For example, surfaces that allow
for solution dripping can pose environmental and operator hazards. Typically, Type
II CCCs must remain in contact with a surface for up to 20 minutes to react. Touch-ups
are often applied by applicator pens, which minimize solution dripping and operator
exposure. However, because the liquid dries quickly, multiple applications are required.
Furthermore, non-drip applicator pens are not available for all coating and solution
options. A need exists for improved Type II CCCs that allow for on-wing repair while
minimizing environmental and operator risks.
SUMMARY
[0003] In one aspect, a spray foam chemical conversion coating includes a non-hexavalent
chromium aqueous chemical conversion coating solution, a foaming agent, and a propellant.
[0004] In another aspect, a method of producing a corrosion-resistant coating includes spraying
a foam chemical conversion coating on a surface of a metal substrate, allowing the
foam chemical conversion coating to react with the surface, and removing excess foam
chemical conversion coating from the surface. The foam chemical conversion coating
contains no hexavalent chromium.
[0005] The present summary is provided only by way of example, and not limitation. Other
aspects of the present disclosure will be appreciated in view of the entirety of the
present disclosure, including the entire text, claims and accompanying figures.
BRIEF DESCRIPTION OF THE DRAWINGS
[0006] FIG. 1 is a flow chart depicting a method of producing a corrosion-resistant barrier
coating on a substrate.
[0007] While the above-identified figures set forth embodiments of the present invention,
other embodiments are also contemplated, as noted in the discussion. In all cases,
this disclosure presents the invention by way of representation and not limitation.
It should be understood that numerous other modifications and embodiments can be devised
by those skilled in the art, which fall within the scope of the principles of the
invention. The figures may not be drawn to scale, and applications and embodiments
of the present invention may include features, steps and/or components not specifically
shown in the drawings.
DETAILED DESCRIPTION
[0008] The present disclosure provides improved application of CCCs that allows for on-wing
repair while minimizing environmental and operator risks. As described further herein,
a foaming agent and propellant can be incorporated into an aqueous CCC to create a
spray foam CCC (also referred to herein as "spray foam conversion coating" or "foam
conversion coating") that can be locally applied and can remain in place without drippage
for at least a time period (e.g. 1-20 minutes) needed to allow for reaction at a surface
of a substrate to produce a barrier coating on the surface of the substrate. The spray
foam conversion coating can permit complex shapes to be coated on-wing or in other
manufacturing locations, without the need for a special environmentally controlled
area, can reduce or eliminate the need for multiple applications as is required with
conventional applicator pens, and can confine the chemical reaction to a specific
location thereby preventing contamination or damage to other surfaces or components.
The resultant coating can provide barrier protection of the substrate in corrosive
environments and can increase a bond strength between the substrate and a primer or
other organic coating. Additionally, the barrier coating can form a thin film allowing
for electrical conductivity.
[0009] As used herein, the term "spray foam" refers to an improved method of applying a
CCC to a substrate and is not used to characterize the resulting coating obtained
using the disclosed method. The physical and chemical properties of the resulting
barrier coating are consistent with those provided by other known methods (e.g., immersion,
applicator pens, brush-on, wipe-on) of applying CCCs. Furthermore, it will be understood
by one of ordinary skill in the art that the present disclosure is not limited to
a particular chemical conversion coating chemistry and can include any aqueous chemical
conversion coating known in the art.
[0010] The spray foam conversion coating includes a non-hexavalent aqueous chemical conversion
coating solution such as a trivalent chromium conversion coating. Various aqueous
trivalent chromium conversion coatings are commercially available, including but not
limited to Chemeon
® eTCP, Chemeon
® TCP-HF, Socosurf TCS, SurTec
® 650 ChromitAL
® TCP, SurTec
® 650V ChromitAL
® TCP, SurTec
® 650C ChromitAL
® TCP, and Alodine
® T5900RTU, BONDERITE
® M-CR T5900 AERO. While the application specifically discloses MIL-DTL-81706 Type
II CCCs used for aluminum substrates, it will be understood by one of ordinary skill
in the art that the aqueous chemical conversion coating solution can include other
aqueous chemical conversion solutions known in the art for application on other metal
substrates (e.g., zinc, cadmium, copper, silver, magnesium, tin, iron, or alloys thereof).
[0011] The aqueous chemical conversion coating solution is mixed with a foaming agent used
to facilitate the formation of foam. The foaming agent is an inert additive that does
not chemically react with the aqueous chemical conversion coating solution or the
substrate. The foaming agent can include one or more chemicals. The foaming agent
can be an anionic alkyl sulfate surfactant such as, sodium laureth sulfate, sodium
lauryl ether sulfate, sodium dodecyl sulfate, ammonium lauryl sulfate. In other embodiments,
the foaming agent can be triethanolamine used alone or in combination with other surfactants
or foaming agents. Surfactants can promote wetting of the substrate surface. Other
suitable foaming agents may include blowing agents, which form the gaseous part of
the foam. Blowing agents can include gases at the temperature the foam is formed (e.g.,
carbon dioxide) or gases generated by chemical reaction (e.g., baking powder, sodium
bicarbonate, ammonium carbonate, ammonium bicarbonate, calcium azide, azodicarbonamide,
titanium hydride, and isocyanates when they react with water). The foaming agent can
be selected to provide a stable foam for a desired reaction time (e.g., 1-20 minutes)
on all surface orientations, including vertically-oriented and overhead surfaces and
to provide bubbles that are too small to interfere with coating formation on the surface
of the substrate.
[0012] Additional chemical constituents may be added to provide a desired foam consistency.
For example, fatty acids such as myristic acid, palmitic acid or steric acid combined
with triethanolamine may be used to thicken the foam or increase stability.
[0013] In one example, the spray foam conversion coating can include a mixture of approximately
6.2 to 10.2 weight percent stearic acid, 2.7 to 4.7 weight percent triethanolamine,
and 86 to 90 weight percent of commercially available non-hexavalent chromium aqueous
conversion coating solution. The commercially available non-hexavalent chromium aqueous
conversion coating solution can be made-up per the manufacturer's recommendation and
combined in the appropriate amount to make up 86 to 90 weight percent of the total
spray foam conversion coating mixture. The pH of the mixture can be adjusted to meet
a pH recommended for use of the commercially available non-hexavalent chromium aqueous
conversion coating solution. The pH may be raised by using sodium hydroxide, potassium
hydroxide, sodium bicarbonate, ammonium carbonate, ammonium bicarbonate. The pH may
be lowered by the addition of stearic acid or sulfuric acid. The properly balanced
pH mixture can then be inserted into a container and mixed with a propellant to achieve
the desired pressurization to expel the mixture.
[0014] In another example, the spray foam conversion coating can include approximately 6.2
to 10.2 weight percent myristic acid or palmitic acid in place of stearic acid. In
another example, approximately 6.2 to 10.2 weight percent of the spray foam conversion
coating can include any combination of two or more of stearic acid, myristic acid,
and palmitic acid.
[0015] In another example, the spray foam conversion coating can include a combination of
foaming agents. For example, approximately 2.7 to 4.7 weight percent of the spray
foam conversion coating can include a combination of triethanolamine and any one or
more anionic alkyl sulfates, such as sodium laureth sulfate, sodium lauryl ether sulfate,
sodium dodecyl sulfate, ammonium lauryl sulfate.
[0016] In one example, the spray foam conversion coating mixture can be formed by heating
the fatty acid(s) (stearic acid, myristic acid, palmitic acid, or any combination
thereof) to a temperature of approximately 179 to 188 degrees Fahrenheit for approximately
40 minutes or until smooth. The fatty acid(s) can be mixed while heating. The fatty
acid(s) can be allowed to cool to about 152 degrees Fahrenheit before adding the remaining
components. The aqueous chemical conversion coating solution and triethanolamine and/or
additional surfactants can be added to the cooled fatty acid(s) and mixed. Mixing
can continue while the mixture cools to form a thick liquid. The thick liquid can
be forced through a screen (e.g., stainless steel screen) to remove lumps and poured
into a container that can be pressurized.
[0017] The spray foam conversion coating includes a compressible propellant capable of expanding
upon release from a pressurized vessel. The propellant can include, for example carbon
dioxide, nitrogen, air or similar non-flammable compressible gases. In some examples,
the propellant can be a flammable propellant such as butane, isobutane, or propane.
In some examples, the propellant can also act as a foaming agent.
[0018] The spray foam conversion coating can be contained in a pressurized vessel, such
as a metal can with a spray nozzle. Any vessel capable of containing the pressurized
gas and liquid materials disclosed herein can be suitable for delivering the spray
foam conversion coating. A handheld can with an operator-triggered delivery mechanism
may be suitable for most repair applications. An interior of the vessel can be formed
of a material that does not react with constituents of the foam conversion coating
to prevent corrosion and leakage and extend a shelf-life of the product. For example,
an aluminum can may be lined with polytetrafluoroethylene (PTFE), bisphenol A (BPA),
polypropylene, or similar material. A liner material can be the same as a material
used to store the aqueous chemical conversion coating solution without the foaming
agent and propellant.
[0019] The spray foam conversion coating mixture can be poured into the open can. A valve
and cover can be fitted onto the can to form a seal and the propellant can be forced
into the can through the valve. In some examples, the can contains approximately 4
to 5 volume percent propellant. A larger amount of propellent could dry the spray
foam corrosion coating mixture as it comes out of the can, rendering it unusable.
[0020] FIG. 1 a flow chart depicting method 10 of producing a corrosion-resistant barrier
coating on a substrate. Method 10 includes applying the spray foam conversion coating
to a surface of a substrate (step 12), allowing the aqueous chemical conversion coating
solution to react with the substrate surface (step 14), and removing the unreacted
or excess foam conversion coating from the surface after this reaction is complete
(step 16).
[0021] The spray foam conversion coating can be applied to a metal substrate that is pretreated
to deoxidize or expose the surface of the metal. The metal substrate can be aluminum
or an aluminum alloy. In some embodiments, the metal substrate can be zinc, cadmium,
copper, silver, magnesium, tin, iron, or alloys thereof. It will be understood by
one of ordinary skill in the art that the type of aqueous conversion coating solution
present in the spray foam conversion coating can be used to determine the application
for which the spray foam conversion coating is best suited. Pre-treatment can include
chemical and or mechanical surface preparation as known in the art. A chemical pre-treatment
can include, for example, degreasing with an alkaline degreaser or solvent, such as
acetone or isopropanol, rinsing with water, and using an acid cleaner, such as nitric
acid, to de-oxidize the surface of the metal substrate. Mechanical pre-treatment can
include, for example, grit-blasting, sanding, pumice scrubbing, or abrasive pad processing
of the metal substrate, which can be followed by degreasing.
[0022] Following surface preparation of the substrate, the spray foam conversion coating
can be applied to a wipe or directly to the surface of the substrate via spraying.
For example, the spray foam conversion coating can be contained in a handheld spray
can with a pressure-triggered spray mechanism (e.g., nozzle or trigger can be pressed
by the operator to release contents of the spray can through the nozzle). Various
spray devices and nozzles known in the art may be suitable for applying the foam conversion
coating and can include both handheld sprayers and robotic or remote-operated devices.
In some applications, it may be advantageous to spray the foam conversion coating
directly to the substrate surface to be coated. In other applications, it may be difficult
to spray directly onto the substrate surface without risking contact with materials
surrounding the substrate surface and, therefore, it may be advantageous to apply
the spray foam conversion coating to a wipe or tool for hand-held application to the
substrate surface. Regardless of the application method, once applied, the foam can
remain in place for a time needed for chemical reaction between the aqueous conversion
coating and the substrate and, therefore, frequent reapplication is not required.
[0023] The spray nozzle can be configured to confine the foam conversion coating to small
region of the substrate surface, for example, a diameter ranging from about 1 to 10
cm or surface area ranging from 0.78 to 78.6 cm
2. The spray can be any of a variety of shapes known in the art and the spray can be
applied from a distance of 1 to 25 cm. Typically, the spray foam conversion coating
can be used to repair a single line scratch on a surface or a nominal marking on a
surface where the original coating has been removed due to damage. It will be understood
by one of ordinary skill in the art that the spray nozzle can be designed as appropriate
for the application. The spray foam conversion coating can permit complex shapes to
be coated on-wing or in other manufacturing locations, without the need for a special
environmentally controlled area. In some examples, the spray foam conversion coating
may need to be applied locally to complex shapes during the normal course of manufacture
or repair. For example, surfaces occasionally get damaged after leaving the coating
facility or during post conversion coating processes (e.g., machining) during manufacture
of a component. It may be desirable to touch up the coating in damaged areas without
the need for transferring the component back to a coating facility.
[0024] Once the foam conversion coating has been applied to the surface of the substrate,
the foam conversion coating is left in place to allow the chemical reaction between
the aqueous chemical conversion coating solution and the metal substrate to occur.
The foam conversion coating remains wet for a period of time that meets or exceeds
the time needed for sufficient chemical reaction to occur (e.g., up to 20 minutes).
Ions (e.g., chromium ions) of the aqueous chemical conversion coating solution can
migrate toward the surface of the substrate while the foam conversion coating remains
on the substrate. Reaction with ions within the foam conversion coating on surface
of the substrate creates an oxide complex (e.g., aluminum chromium oxide complex)
on the surface of the substrate, thereby changing the bare metal into a new, intentionally
deposited, selective oxide layer that provides a barrier coating to prevent corrosion
and oxidation of the substrate.
[0025] A single application of the foam conversion coating can be sufficient for repair
or reconditioning of the substrate. The foam conversion coating does not have to be
continuously reapplied to ensure formation of the selective oxide layer. The chemical
reaction can continue to occur for as long as the foam conversion coating is on the
substrate provided the foam conversion coating does not dry. The reaction time can
typically range from about 1 minute to about 20 minutes depending on the particular
chemistry of the aqueous chemical conversion coating solution. In some environments
(e.g., coating applied in the sun), the foam conversion coating may be susceptible
to drying and may require mixing or agitating on the surface to ensure the aqueous
portion of the foam conversion coating remains in contact with the surface. Additional
applications of the foam conversion coating would be permitted in environments where
unintentional drying occurs.
[0026] The excess or unreacted foam conversion coating is removed from the substrate following
a time period determined suitable for chemical reaction (e.g., 1-20 minutes). The
foam conversion coating can be removed by wiping the substrate surface with a moist
and/or dry wipe (e.g., moist or dry cloth) and disposed of in accordance with local
environmental regulations for the aqueous chemical conversion coating solution. Any
remaining foam, particularly, inert components of the foam conversion coating, can
be removed, for example, with a water-wetted cloth (e.g., microfiber) or other non-abrasive
material. Generally, wipes should not contain materials other than water. Wipes containing
surfactants or oils could contaminate the surface. Wipes containing solvents could
chemically dehydrate the surface during the curing process. Care should be taken to
avoid abrading the coating. Any remaining aqueous chemical conversion coating solution
can dry in place. The resulting barrier coating does not require post-treatment. The
coated substrate can be ready for use once the excess foam has been removed from the
surface and the remaining aqueous chemical conversion coating solution has dried.
In some embodiments, a primer and or other organic coating can be applied to the barrier
coating.
[0027] In some embodiments, the spray foam conversion coating can include a visual indicator
(e.g., red to violet coloring) as known in the art to confirm presence of the barrier
coating on the surface upon inspection after the excess foam has been removed and
any remaining aqueous conversion coating has dried.
[0028] The disclosed spray foam conversion coating provides a thin film barrier coating
having a thickness, for example, of approximately 380 nanometres (15 millionths of
an inch), allowing for electrical conductivity.
[0029] The disclosed spray foam conversion coating can be used to coat any substrate or
component subject to corrosion, for example, aluminum components including propeller
blades, gear box housings, heat exchangers, electronic fuel control housings, brackets,
air cycle machines, turbine blades, valve bodies, aircraft structural body frames,
aircraft body panels, and aircraft wheels, among others. While the majority of the
examples listed apply to aircraft components, it will be understood that the disclosed
spray foam conversion coating can be applied to any metal structure requiring a locally
applied conversion coating.
[0030] The disclosed spray foam conversion coating can be used for touch-up repair of aircraft
surfaces on-wing or on parts that have been removed from the aircraft for reconditioning.
The spray foam conversion coating can allow for repair of multiple aircraft parts
and surfaces, including difficult-to-reach surfaces, vertical surfaces, and overhead
surfaces.
[0031] It will be understood by one of ordinary skill in the art that the disclosed foam
conversion coating is not limited to aerospace applications and can be used in a variety
of applications where chemical conversion coatings are useful. Furthermore, the disclosed
foam conversion coating can be used to deliver any known aqueous chemical conversion
coating solution and is not limited to the chemical conversion coatings disclosed
herein. It will be understood that the disclosed foaming agents and propellants can
be mixed with a wide variety of chemical conversion coatings to improve delivery of
the chemical conversion coating to a surface and provide particular benefit for localized
repair applications.
[0032] Any relative terms or terms of degree used herein, such as "substantially", "essentially",
"generally", "approximately" and the like, should be interpreted in accordance with
and subject to any applicable definitions or limits expressly stated herein. In all
instances, any relative terms or terms of degree used herein should be interpreted
to broadly encompass any relevant disclosed embodiments as well as such ranges or
variations as would be understood by a person of ordinary skill in the art in view
of the entirety of the present disclosure, such as to encompass ordinary manufacturing
tolerance variations, incidental alignment variations, transient alignment or shape
variations induced by thermal, rotational or vibrational operational conditions, and
the like. Moreover, any relative terms or terms of degree used herein should be interpreted
to encompass a range that expressly includes the designated quality, characteristic,
parameter or value, without variation, as if no qualifying relative term or term of
degree were utilized in the given disclosure or recitation.
Discussion of Possible Embodiments
[0033] The following are non-exclusive descriptions of possible embodiments of the present
invention.
[0034] A spray foam chemical conversion coating includes a non-hexavalent chromium aqueous
chemical conversion coating solution, a foaming agent, and a propellant.
[0035] The spray foam chemical conversion coating of the preceding paragraph can optionally
include, additionally and/or alternatively, any one or more of the following features,
configurations and/or additional components:
[0036] The spray foam chemical conversion coating of the preceding paragraphs, wherein the
aqueous chemical conversion coating solution comprises trivalent chromium.
[0037] The spray foam chemical conversion coating of any of the preceding paragraphs, wherein
the foaming agent does not react with the aqueous chemical conversion coating solution
or the surface to be coated.
[0038] The spray foam chemical conversion coating of any of the preceding paragraphs, wherein
the foaming agent is a surfactant.
[0039] The spray foam chemical conversion coating of any of the preceding paragraphs, wherein
the foaming agent is selected from the group consisting of triethanolamine, sodium
laureth sulfate, sodium lauryl ether sulfate, sodium dodecyl sulfate, and ammonium
lauryl sulfate.
[0040] The spray foam chemical conversion coating of any of the preceding paragraphs, wherein
the spray foam chemical conversion coating comprises approximately 2.7 to 4.7 weight
percent foaming agent.
[0041] The spray foam chemical conversion coating of any of the preceding paragraphs, wherein
the propellent is non-flammable.
[0042] The spray foam chemical conversion coating of any of the preceding paragraphs, and
further comprising a fatty acid selected from the group consisting of stearic acid,
myristic acid, palmitic acid, and combinations thereof.
[0043] The spray foam chemical conversion coating of any of the preceding paragraphs, wherein
the spray foam chemical conversion coating is contained under pressure until applied
via spraying.
[0044] A method of producing a corrosion-resistant coating includes spraying a foam chemical
conversion coating on a surface of a metal substrate, allowing the foam chemical conversion
coating to react with the surface, and removing excess foam chemical conversion coating
from the surface. The foam chemical conversion coating contains no hexavalent chromium.
[0045] The method of the preceding paragraph can optionally include, additionally and/or
alternatively, any one or more of the following features, configurations, additional
components, and/or steps:
[0046] The method of the preceding paragraphs, wherein the foam chemical conversion coating
includes an aqueous chemical conversion coating solution, a foaming agent, and a propellant.
[0047] The method of any of the preceding paragraphs, wherein the aqueous chemical conversion
coating solution comprises trivalent chromium.
[0048] The method of any of the preceding paragraphs, wherein the foaming agent is a surfactant.
[0049] The method of any of the preceding paragraphs, wherein the surfactant is selected
from the group consisting of triethanolamine, sodium laureth sulfate, sodium lauryl
ether sulfate, sodium dodecyl sulfate, and ammonium lauryl sulfate.
[0050] The method of any of the preceding paragraphs, wherein the spray foam chemical conversion
coating comprises approximately 2.7 to 4.7 weight percent foaming agent.
[0051] The method of any of the preceding paragraphs, wherein the period of time ranges
from 1 to 20 minutes.
[0052] The method of any of the preceding paragraphs, wherein removing the foam chemical
conversion coating comprises wiping the foam chemical conversion coating from the
surface with a water-wetted wipe.
[0053] The method of any of the preceding paragraphs, wherein the foam chemical conversion
coating is contained under pressure until sprayed.
[0054] The method of any of the preceding paragraphs, wherein the metal substrate is selected
from the group consisting of aluminum, zinc, cadmium, copper, silver, magnesium, tin,
iron, aluminum based alloys, zinc based alloys, cadmium based alloys, copper based
alloys, silver based alloys, magnesium based alloys, iron based alloys, and tin based
alloys.
[0055] The method of any of the preceding paragraphs, and further comprising pre-treating
the metal substrate such that the surface of the metal substrate is deoxidized.
[0056] While the invention has been described with reference to an exemplary embodiment(s),
it will be understood by those skilled in the art that various changes may be made,
and equivalents may be substituted for elements thereof without departing from the
scope of the invention. In addition, many modifications may be made to adapt a particular
situation or material to the teachings of the invention without departing from the
essential scope thereof. Therefore, it is intended that the invention not be limited
to the particular embodiment(s) disclosed, but that the invention will include all
embodiments falling within the scope of the appended claims.
1. A spray foam chemical conversion coating comprising:
a non-hexavalent chromium aqueous chemical conversion coating solution;
a foaming agent; and
a propellant.
2. The spray foam chemical conversion coating of claim 1, wherein the aqueous chemical
conversion coating solution comprises trivalent chromium.
3. The spray foam chemical conversion coating of claim 1 or 2, wherein the foaming agent
does not react with the aqueous chemical conversion coating solution or the surface
to be coated.
4. The spray foam chemical conversion coating of any preceding claim, wherein the foaming
agent is a surfactant.
5. The spray foam chemical conversion coating of any preceding claim, wherein the foaming
agent is selected from the group consisting of triethanolamine, sodium laureth sulfate,
sodium lauryl ether sulfate, sodium dodecyl sulfate, and ammonium lauryl sulfate.
6. The spray foam chemical conversion coating of any preceding claim, wherein the spray
foam chemical conversion coating comprises approximately 2.7 to 4.7 weight percent
foaming agent; and/or, wherein the propellent is non-flammable.
7. The spray foam chemical conversion coating of any preceding claim, further comprising
a fatty acid selected from the group consisting of stearic acid, myristic acid, palmitic
acid, and combinations thereof; and/or
wherein the spray foam chemical conversion coating is contained under pressure until
applied via spraying.
8. A method of producing a corrosion-resistant coating, the method comprising:
spraying a foam chemical conversion coating on a surface of a metal substrate;
allowing the foam chemical conversion coating to react with the surface; and
removing excess foam chemical conversion coating from the surface;
wherein the foam chemical conversion coating contains no hexavalent chromium.
9. The method of claim 8, wherein the foam chemical conversion coating comprises:
an aqueous chemical conversion coating solution;
a foaming agent; and
a propellant; and optionally
wherein the aqueous chemical conversion coating solution comprises trivalent chromium.
10. The method of claim 9, wherein the foaming agent is a surfactant; and optionally,
wherein the surfactant is selected from the group consisting of triethanolamine, sodium
laureth sulfate, sodium lauryl ether sulfate, sodium dodecyl sulfate, and ammonium
lauryl sulfate.
11. The method of any of claims 8 to 10, wherein the spray foam chemical conversion coating
comprises approximately 2.7 to 4.7 weight percent foaming agent.
12. The method of any of claims 8 to 11, wherein the period of time ranges from 1 to 20
minutes.
13. The method of any of claims 8 to 12, wherein removing the foam chemical conversion
coating comprises wiping the foam chemical conversion coating from the surface with
a water-wetted wipe; and/or, wherein the foam chemical conversion coating is contained
under pressure until sprayed.
14. The method of any of claims 8 to 13, wherein the metal substrate is selected from
the group consisting of aluminum, zinc, cadmium, copper, silver, magnesium, tin, iron,
aluminum based alloys, zinc based alloys, cadmium based alloys, copper based alloys,
silver based alloys, magnesium based alloys, iron based alloys, and tin based alloys.
15. The method of any of claims 8 to 14, and further comprising pre-treating the metal
substrate such that the surface of the metal substrate is deoxidized.